MEDLIB
Orphanet Database

Редкие заболевания

7,547 заболеваний с генами, фенотипами и эпидемиологией

7,547Болезней
4 552Генов
8 700Фенотипов

Feingold syndrome type 2

ORPHA:391646Клин. подтип
Autosomal dominant

Felty syndrome

ORPHA:47612Заболевание
Unknown

Female infertility due to oocyte meiotic arrest

ORPHA:488191Заболевание
Autosomal recessive

Female infertility due to zona pellucida defect

ORPHA:404466Заболевание
Autosomal dominant, Autosomal recessive

Femoral-facial syndrome

ORPHA:1988Мальформация
Not applicable

Femur-fibula-ulna complex

ORPHA:2019Мальформация
Not applicable

Ferro-cerebro-cutaneous syndrome

ORPHA:397922Заболевание
X-linked recessive

Ferroportin disease

ORPHA:648562Заболевание

Fetal Gaucher disease

ORPHA:85212Клин. подтип
Autosomal recessive

Fetal akinesia deformation sequence

ORPHA:994Мальформация
Autosomal recessive

Fetal akinesia-cerebral and retinal hemorrhage syndrome

ORPHA:363409Заболевание
Autosomal recessive

Fetal alcohol syndrome

ORPHA:1915Мальформация
Not applicable

Fetal and neonatal alloimmune thrombocytopenia

ORPHA:853Заболевание
Not applicable

Fetal carbamazepine syndrome

ORPHA:370076Мальформация
Not applicable

Fetal cytomegalovirus syndrome

ORPHA:294Заболевание
Not applicable

Fetal encasement syndrome

ORPHA:465824Мальформация
Autosomal recessive

Fetal hydantoin syndrome

ORPHA:1912Мальформация
Not applicable

Fetal iodine syndrome

ORPHA:1910Мальформация
Not applicable

Fetal lung interstitial tumor

ORPHA:284362Клин. подтип

Fetal methylmercury syndrome

ORPHA:1917Мальформация
Not applicable

Fetal minoxidil syndrome

ORPHA:1918Мальформация
Not applicable

Fetal parvovirus syndrome

ORPHA:295Мальформация
Not applicable

Fetal trimethadione syndrome

ORPHA:1913Мальформация
Not applicable

Fetal valproate spectrum disorder

ORPHA:1906Мальформация
Not applicable